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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098575copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,149,173-85,166,363 , GRCh38.p12 chrX: 85,894,168-85,911,358 CHM, MIR361
    nsv7098554copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,223,644 , GRCh38.p12 chrX: 85,864,630-85,968,639 CHM, MIR361
    nsv7098337copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,302,644 , GRCh38.p12 chrX: 85,864,630-86,047,640 MIR361, CHM
    nsv7098336copy number variation1nstd102humanUncertain significance GRCh37 chrX: 84,600,846-85,302,644 , GRCh38.p12 chrX: 85,345,840-86,047,640 CHM, SFR1P2, 3 more genes
    nsv7090104copy number variation1nstd229human GRCh38 chrX: 85,899,101-85,906,300 , GRCh37.p13 chrX: 85,154,106-85,161,305 MIR361, CHM
    nsv7090103copy number variation1nstd229human GRCh38 chrX: 85,899,001-85,908,200 , GRCh37.p13 chrX: 85,154,006-85,163,205 CHM, MIR361
    nsv7090102copy number variation1nstd229human GRCh38 chrX: 85,899,001-85,906,400 , GRCh37.p13 chrX: 85,154,006-85,161,405 MIR361, CHM
    nsv7090095copy number variation1nstd229human GRCh38 chrX: 85,838,959-85,996,906 , GRCh37.p13 chrX: 85,093,964-85,251,910 MIR361, CHM, 1 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313469copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,104,966-86,189,374 , GRCh38.p12 chrX: 78,849,469-86,934,371 MIR361, TERF1P4, 59 more genes
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 more genes
    nsv6313383copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,302,634 , GRCh38.p12 chrX: 85,864,630-86,047,630 CHM, MIR361
    nsv6290670copy number variation1nstd102humanUncertain significance GRCh37 chrX: 78,558,916-86,314,970 , GRCh38.p12 chrX: 79,303,419-87,059,967 LOC105373284, RNU6-995P, 54 more genes
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